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Maturity-onset diabetes of the young type 9 or latent autoimmune diabetes in adults: A case report and review of literature

BACKGROUND: Maturity-onset diabetes of the young (MODY) is a monogenic genetic disease often clinically misdiagnosed as type 1 or type 2 diabetes. MODY type 9 (MODY9) is a rare subtype caused by mutations in the PAX4 gene. Currently, there are limited reports on PAX4-MODY, and its clinical character...

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Autores principales: Zhou, Guang-Hong, Tao, Min, Wang, Qing, Chen, Xing-Yu, Liu, Jing, Zhang, Li-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10401456/
https://www.ncbi.nlm.nih.gov/pubmed/37547587
http://dx.doi.org/10.4239/wjd.v14.i7.1137
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author Zhou, Guang-Hong
Tao, Min
Wang, Qing
Chen, Xing-Yu
Liu, Jing
Zhang, Li-Li
author_facet Zhou, Guang-Hong
Tao, Min
Wang, Qing
Chen, Xing-Yu
Liu, Jing
Zhang, Li-Li
author_sort Zhou, Guang-Hong
collection PubMed
description BACKGROUND: Maturity-onset diabetes of the young (MODY) is a monogenic genetic disease often clinically misdiagnosed as type 1 or type 2 diabetes. MODY type 9 (MODY9) is a rare subtype caused by mutations in the PAX4 gene. Currently, there are limited reports on PAX4-MODY, and its clinical characteristics and treatments are still unclear. In this report, we described a Chinese patient with high autoimmune antibodies, hyperglycemia and a site mutation in the PAX4 gene. CASE SUMMARY: A 42-year-old obese woman suffered diabetes ketoacidosis after consuming substantial amounts of beverages. She had never had diabetes before, and no one in her family had it. However, her autoantibody tested positive, and she managed her blood glucose within the normal range for 6 mo through lifestyle inter-ventions. Later, her blood glucose gradually increased. Next-generation sequencing and Sanger sequencing were performed on her family. The results revealed that she and her mother had a heterozygous mutation in the PAX4 gene (c.314G>A, p.R105H), but her daughter did not. The patient is currently taking liraglutide (1.8 mg/d), and her blood glucose levels are under control. Previous cases were retrieved from PubMed to investigate the relationship between PAX4 gene mutations and diabetes. CONCLUSION: We reported the first case of a PAX4 gene heterozygous mutation site (c.314G>A, p.R105H), which does not appear pathogenic to MODY9 but may facilitate the progression of latent autoimmune diabetes in adults.
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spelling pubmed-104014562023-08-05 Maturity-onset diabetes of the young type 9 or latent autoimmune diabetes in adults: A case report and review of literature Zhou, Guang-Hong Tao, Min Wang, Qing Chen, Xing-Yu Liu, Jing Zhang, Li-Li World J Diabetes Case Report BACKGROUND: Maturity-onset diabetes of the young (MODY) is a monogenic genetic disease often clinically misdiagnosed as type 1 or type 2 diabetes. MODY type 9 (MODY9) is a rare subtype caused by mutations in the PAX4 gene. Currently, there are limited reports on PAX4-MODY, and its clinical characteristics and treatments are still unclear. In this report, we described a Chinese patient with high autoimmune antibodies, hyperglycemia and a site mutation in the PAX4 gene. CASE SUMMARY: A 42-year-old obese woman suffered diabetes ketoacidosis after consuming substantial amounts of beverages. She had never had diabetes before, and no one in her family had it. However, her autoantibody tested positive, and she managed her blood glucose within the normal range for 6 mo through lifestyle inter-ventions. Later, her blood glucose gradually increased. Next-generation sequencing and Sanger sequencing were performed on her family. The results revealed that she and her mother had a heterozygous mutation in the PAX4 gene (c.314G>A, p.R105H), but her daughter did not. The patient is currently taking liraglutide (1.8 mg/d), and her blood glucose levels are under control. Previous cases were retrieved from PubMed to investigate the relationship between PAX4 gene mutations and diabetes. CONCLUSION: We reported the first case of a PAX4 gene heterozygous mutation site (c.314G>A, p.R105H), which does not appear pathogenic to MODY9 but may facilitate the progression of latent autoimmune diabetes in adults. Baishideng Publishing Group Inc 2023-07-15 2023-07-15 /pmc/articles/PMC10401456/ /pubmed/37547587 http://dx.doi.org/10.4239/wjd.v14.i7.1137 Text en ©The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Case Report
Zhou, Guang-Hong
Tao, Min
Wang, Qing
Chen, Xing-Yu
Liu, Jing
Zhang, Li-Li
Maturity-onset diabetes of the young type 9 or latent autoimmune diabetes in adults: A case report and review of literature
title Maturity-onset diabetes of the young type 9 or latent autoimmune diabetes in adults: A case report and review of literature
title_full Maturity-onset diabetes of the young type 9 or latent autoimmune diabetes in adults: A case report and review of literature
title_fullStr Maturity-onset diabetes of the young type 9 or latent autoimmune diabetes in adults: A case report and review of literature
title_full_unstemmed Maturity-onset diabetes of the young type 9 or latent autoimmune diabetes in adults: A case report and review of literature
title_short Maturity-onset diabetes of the young type 9 or latent autoimmune diabetes in adults: A case report and review of literature
title_sort maturity-onset diabetes of the young type 9 or latent autoimmune diabetes in adults: a case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10401456/
https://www.ncbi.nlm.nih.gov/pubmed/37547587
http://dx.doi.org/10.4239/wjd.v14.i7.1137
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